Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: SNX2 ENSBTAG00000025358

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Description

sorting nexin 2 [Source:VGNC Symbol;Acc:VGNC:35100]

Location

Primary_assembly 7: 30,993,858-31,052,612 reverse strand.

ARS-UCD2.0:CM008174.2

About this gene

This gene has 2 transcripts (splice variants), 209 orthologues and 15 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000035582.4	SNX2-201	2039	519aa	ENSBTAP00000035453.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MZN7	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSBTAT00000120516.1	SNX2-202	1958	492aa	ENSBTAP00000083818.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SEJ5	-

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Summary

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